Which one of among the following genetic profile I could possibly belong to the father of the child
Answers
Answer:
Genetic testing can help doctors look for missing or defective genes. This information helps them know if a person, their partner, or their baby is likely to have certain medical conditions.
Genetic tests are when small samples of blood or body tissues are analyzed. Many different types of body fluids and tissues can be used. The type of genetic test needed to make a diagnosis depends on which condition a doctor checks for.
Explanation:
Why Do Doctors Recommend Genetic Testing?
A doctor may recommend genetic counseling or testing for any of these reasons:
The pregnant woman is over age 34. A pregnant woman's chances of having a child with a chromosomal problem (such as trisomy) increase if she is older than 34. Children of older fathers are at risk for new dominant genetic mutations — those caused by a single genetic defect that hasn't run in the family before.
A standard prenatal screening test had an abnormal result. Doctors may recommend genetic testing if a screening test showed a possible genetic problem.
A couple plans to start a family and one of them or a close relative has an inherited illness. Some people are carriers of genes for genetic illnesses, even though they don't show signs of the illness themselves. This happens because some genetic illnesses are recessive. This means they cause symptoms only if a person inherits two copies of the problem gene, one from each parent. Children who inherit one problem gene from one parent but a normal gene from the other parent won't have symptoms of a recessive illness. But they will have a 50% chance of passing the problem gene to their children.
A parent already has one child with a serious birth defect. Not all children who have birth defects have genetic problems. Sometimes, exposure to a toxin (poison), infection, or physical trauma before birth causes a birth defect. Often, the cause isn't known. Even if a child has a genetic problem, it might not have been inherited. Some happen because of a spontaneous error in the child's cells, not the parents' cells.
A woman has had two or more miscarriages. Severe chromosome problems in the fetus can sometimes lead to a spontaneous miscarriage. Several miscarriages may point to a genetic problem.
A woman has delivered a stillborn child with physical signs of a genetic illness. Many serious genetic illnesses cause specific and distinctive physical problems.
A child has medical problems that might be genetic. When a child has medical problems involving more than one body system, genetic testing might help doctors find the cause and make a diagnosis.
A child has medical problems known to be part of a genetic syndrome. Genetic testing can confirm the diagnosis. In some cases, it also might help find the type or severity of a genetic illness. This can help doctors find the best treatment.
Which one of among the following genetic profile I could possibly belong to the father of the child